Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maha K Alghamdi"'
Inflammatory bowel disease in the elderly: A focus on disease characteristics and treatment patterns
Autor:
Mahmoud H Mosli, Maha K Alghamdi, Omar A Bokhary, Maria A Alzahrani, Siba Z Takieddin, Tala A Galai, Majid A Alsahafi, Omar I Saadah
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 29, Iss 4, Pp 212-218 (2023)
Background: As the population ages, the number of elderly inflammatory bowel disease (IBD) patients is expected to increase. The clinical features and therapeutic options for young and old patients may differ, as elderly IBD patients are likely to ha
Externí odkaz:
https://doaj.org/article/e09bd4a8df494d4e92a861616c93a2a8
Autor:
Maha K Alghamdi, Hanadi M Alhozali, Omar A Bokhary, Renad A Ahmed, Abdulrahman A Alghamdi, Wejdan S Almalki, Omar A Almutairi
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 10, Iss 3, Pp 221-226 (2022)
Background: Acute kidney injury (AKI) is associated with an increase in patient mortality and high rates of renal/non-renal complications. Late detection of the disease has been associated with worse prognosis, but no such study has been conducted fr
Externí odkaz:
https://doaj.org/article/9d4579675e6f454d89ac53fbc9f90ddd
Autor:
Nouran H Farag, Zahraa H Alsaggaf, Noha O Bamardouf, Dhuha M Khesfaty, Morouj M Fatani, Maha K Alghamdi, Samah N Saharti
Publikováno v:
Cureus.
Autor:
Imad M Khojah, Maha K Alghamdi, Bassam M Alahmari, Maria A Alzahrani, Hassan G Alshehri, Jamal S Farahat, Ghada A Merdad, Ahmed Aalam
Publikováno v:
Cureus.
Autor:
Hanadi M Alhozali, Renad A Ahmed, Rasana B Albeirouti, Fahad A Alotibi, Deemah K Ghazi, Mohammad A Shikdar, Maha K Alghamdi, Reem A Al Zahrani
Publikováno v:
Cureus. 14(3)
Background Focal segmental glomerulosclerosis (FSGS) is characterized by the presence of glomerular damage on histopathological examination. The major defining symptom of FSGS is proteinuria, which indicates damage to the glomerular filtration barrie
Autor:
Nour Gazzaz, Maha K. Alghamdi
Publikováno v:
Cureus
Familial hypomagnesemia with secondary hypocalcemia is a rare genetic disorder of magnesium metabolism that presents with refractory seizures during infancy. It is caused by loss-of-function mutations in the gene encoding transient receptor potential
Autor:
Omar A. Bokhary, Hanadi M. Alhozali, Ahmed M. Abulfaraj, Abdulaziz S. Alkhallagi, Abdulmohsen S. Aldharrab, Reem A. Al Zahrani, Maha K. Alghamdi, Faisal S. Alyahya
Publikováno v:
Cureus
Background: Immunoglobulin A nephropathy (IgAN) is the most common primary aetiology of glomerulonephritis worldwide, and it is the most important type in terms of morbidity and mortality. IgAN involves the deposition of immune bodies in the mesangia
Autor:
Imad M. Khojah, Osama Y. Muthaffar, Anas S. Alyazidi, Maha K. Alghamdi, Mayar M. Salem, Hassan A. Alalawi, Ohud T. Alharbi, Latifa A. Almuharib
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 60, Iss 1, Pp 1-7 (2024)
Abstract Background COVID-19 is a global pandemic that has highly impacted the healthcare system and patients, especially patients with epilepsy, due to the fact that the success of their treatment depends on obtaining sustainable access to medical p
Externí odkaz:
https://doaj.org/article/06bf093589f64400a668e81d68711fa7